6 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MECTALIF ANT - LAG
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OVD·April 12, 2024
DURAL ALPHA INSERT NEUTR II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 29, 2025
HEARTSTING III PROXIMAL SEAL SYSTEM
FDA Adverse Event
Malfunction
·GUIDANT CARDIOVASCULAR·Product code DXC·October 31, 2008
PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·September 2, 2011
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·July 18, 2013
ALLOFIT ALLOCLAS SHELL 52/II
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·September 29, 2025